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Our data is continuously updated and sourced from EUDAMED, the European database for medical devices and in vitro diagnostics.

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M118xxx — 7 UDI-DI variants, MDR (ADE Germany GmbH)

MD Atlas
ADE Germany GmbH

Data from EUDAMED, last updated May 23, 2026

M118xxx

426063742000TypeM1185H

7 UDI-DI variants

MDR [Regulation (EU) 2017/745 on medical devices]Class I

Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Manufacturer: ADE Germany GmbH

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Device characteristics

Active deviceMeasuring function

Identity & classification

Basic UDI-DI: 426063742000TypeM1185H
Device name: —
Device model: M118xxx
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: May 18, 2026

Manufacturer & authorised representative

Manufacturer

Name: ADE Germany GmbH
SRN: DE-MF-000005406
Country: Germany
Email: info@ade-germany.de
Phone: +49 40 432 776 - 0

Variants by status

UDI-DI variants

7 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01KRXR57PE6E6ZJRB40XMVMYWJ

Format

Summary

29 columns included

Trade name
Basic UDI-DI
UDI-DI code
Risk category
Applicable legislation
Status
Organization name
SRN
Reference / catalog number
Additional product description
Intended medical purpose
Placed on the market (country)
Market info update date
Sterile
Single use
Contains latex
Reprocessed single-use
Direct marking
CMR substance
Endocrine disruptor
Annex XVI applicable
Sterilization
OEM applicable
EMDN codes
Last updated
Basic UDI-DI device name
Basic UDI-DI device model
Basic UDI-DI implantable
Basic UDI-DI reagent

M118600-0104260637421982
M118000-0104260637428042
M118000-01S04260637428059
M118000S04260637428035
M118600-0204260637425539
M11860004260637421975
M11800004260637428028